HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424745Generated: October 31, 2026
Ethanol → ethyl 2,3-dihydro-1H-indene-2-carboxylate
https://huagongshe.com/reaction/1424745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Indancarboxylic Acid | HCID 575777 | — |
| Product | ethyl 2,3-dihydro-1H-indene-2-carboxylate | HCID 15280733 | — |
Reaction Steps
To a solution of indan-2-carboxylic acid (2.50 g) in ethanol (77 mL) at 25° C. was added concentrated H2SO4 (9 mL). The colorless solution was stirred at 75° C. over a period of 48 h. Solvent was removed under reduced pressure and the residue was diluted with dichloromethane (10 mL) and water (10 mL). The pH of the solution was brought from 1 to 14. Two layers were separated and the aqueous phase was extracted with ethyl acetate (30 mL). Organic layers were combined, dried over magnesium sulfate, filtered and concentrated under high vacuum. The solid obtained was purified on a Biotage™ 40M column (silica, hexanes/ethyl acetate 1:0 to 97:3) to give indan-2-carboxylic acid ethyl ester. Off-white oil; 1H NMR (400 MHz, CDCl3): δ 7.22-7.14 (m, 4H), 4.19 (q, J=7.04 Hz, 4H), 3.36-3.10 (m, 5H), 1.29 (t, J=7.04 Hz, 3H); LRMS (ESI): m/z 190 (MH+); HPLC: 4.3 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927765B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-59c67551baf941e9b27c7b3227419a71 |
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| Source note | uspto-grants-2015_01 |
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